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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408463Generated: October 29, 2026

tert-Butanol → cis-(+/-)-Benzyl 3,5-bis(tert-butoxycarbonylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/408463

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantDiisopropylethylamineHCID 81531—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 86656441HCID 86656441—
Productcis-(+/-)-Benzyl 3,5-bis(tert-butoxycarbonylamino)piperidine-1-carboxylateHCID 5886513323%

Reaction Steps

To a solution of cis-(+/−)-1-(benzyloxycarbonyl)-5-(tert-butoxycarbonylamino) piperidine-3-carboxylic acid (1.2 g, 3.17 mmol), DPPA (Diphenylphosphoryl azide, 1.04 g, 3.81 mmol) and DIEA(1.1 mL, 6.35 mmol) in t-BuOH(10 mL) was heated to 90° C. over night. The solvent was removed under reduced pressure. To the crude was added EtOAc (300 mL), the organic layer was washed with saturated NaHCO3(150 mL) and brine, dried and filtered, and concentrated to give the crude. The crude material was further purified by silica gel chromatography to yielding cis-(+/−)-benzyl 3,5-bis(tert-butoxycarbonylamino)piperidine-1-carboxylate, (23%). LCMS (m/z): 350(minus one Boc(MH+); LC Rt=4.40 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759338B2
Source datasetuspto-grants-2014_06
ORD IDord-331c164243ff4bdd9dc2a1ab69a47293
Source noteuspto-grants-2014_06